Going From A Darzalex Faspro/Revlimid/Dexemetesone Regimen To A Darzalex Only.
I've been on Darzalex Faspro/Revlimid/Dexemetesone for almost 2 years now. One year in we lowered the Rev dose from 25mg to 10mg. Myeloma numbers have continued to look good, so we are considering stopping the Rev altogether at the 2 year mark in April 2023. We will continue with the Darzalex shots and blood tests once a month and see what happens. Anybody have any thoughts on this?
Darzalex, Velcade, and Dexamethasone was the treatment plan I started after the Rev, Velcade and Dex started to keep numbers in check. Eventually I went on Darzalex FastPro alone which was effective for another yr+ before it too began to fail.
I just began daily Rev 10mg with monthly Dara infusion for maintenance post SCT in October ‘22. I was told last month I’m in remission. I’m doing really well especially given that I was in a wheel chair this same time last year.
I too changed from 25 mg Revlimid to 10 mg and with the velcade shots have seen my blood work #s improve over the last 13 months. i will be very interested in any changes your med teams come up with....particularly use of carT transfers...and while you feel good and NOT after 3 or 4 relapses....lets hope the med community decides to use all available options to help/improve our quality of life, now...not just after prior failures
Well, I’ve been in Remission for about a year. Been taking 10ml maintenance REVLIMID. I think I would be scared to come of the REV. 🙃
3 months into first round of the induction phase. My diagnostic markers for MM are almost back to normal. I expect I'll stay on this same regimen awhile. My Dr reduced Rev and steroid once already due to my complaints. Really appreciate your sharing as I know more what to expect.
Mag 🙂
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